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Structure of 150349-65-8
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tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate features a piperidine core functionalized with a primary amine at the C3 position, enabling direct conjugation or further derivatization. The tert-butyl ester group provides stability and facilitates orthogonal deprotection under mild acidic conditions. This scaffold serves as a key intermediate in the synthesis of bioactive molecules, particularly within medicinal chemistry campaigns targeting G protein-coupled receptors.
tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate serves as a versatile bifunctional building block for medicinal chemistry and process development. The piperidine core provides a rigid, basic scaffold ideal for drug discovery, while the pendant primary amine enables conjugation via amidation, alkylation, or reductive amination. The tert-butyl carbamate group offers excellent bench stability and orthogonal protection, facilitating selective deprotection under mild acidic conditions. This compound functions as a key intermediate in the synthesis of bioactive molecules, particularly those requiring extended aliphatic linkers between pharmacophores.
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GHS Pictogram :
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GHS No : GHS07,GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P330-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: